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rs869312051

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312051(G;T)
Make rs869312051(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position178605413
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs869312051
ebirs869312051
HLIrs869312051
Exacrs869312051
Varsomers869312051
Maprs869312051
PheGenIrs869312051
hapmaprs869312051
1000 genomesrs869312051
hgdprs869312051
ensemblrs869312051
gopubmedrs869312051
geneviewrs869312051
scholarrs869312051
googlers869312051
pharmgkbrs869312051
gwascentralrs869312051
openSNPrs869312051
23andMers869312051
23andMe allrs869312051
SNP Nexus

SNPshotrs869312051
SNPdbers869312051
MSV3drs869312051
GWAS Ctlgrs869312051
Max Magnitude0
ClinVar
Risk rs869312051(T;T)
Alt rs869312051(T;T)
Reference rs869312051(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TTN TTN-AS1
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000002.11:g.179470140C>A
CLNSRC
CLNACC RCV000209139.1,